The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
116191612 11619161 2 F 20160613 20151012 20160822 EXP US-ELI_LILLY_AND_COMPANY-US201510000986 ELI LILLY AND CO 0.00 M Y 0.00000 20160822 LW US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
116191612 11619161 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 21427 CAPSULE
116191612 11619161 2 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 21427 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116191612 11619161 1 Pain
116191612 11619161 2 Depression

Outcome of event

Event ID CASEID OUTC COD
116191612 11619161 DE
116191612 11619161 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116191612 11619161 Aggression
116191612 11619161 Agitation
116191612 11619161 Confusional state
116191612 11619161 Death
116191612 11619161 Diarrhoea
116191612 11619161 Disturbance in attention
116191612 11619161 Dizziness
116191612 11619161 Drug withdrawal syndrome
116191612 11619161 Fatigue
116191612 11619161 Hallucination
116191612 11619161 Headache
116191612 11619161 Insomnia
116191612 11619161 Irritability
116191612 11619161 Memory impairment
116191612 11619161 Migraine
116191612 11619161 Mood swings
116191612 11619161 Nausea
116191612 11619161 Nightmare
116191612 11619161 Paraesthesia
116191612 11619161 Sensory disturbance
116191612 11619161 Sleep disorder
116191612 11619161 Suicidal ideation
116191612 11619161 Vertigo

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found